N-Benzyl-4-chloro-1-(4-methylphenyl)-1H-pyrazole-5-carboxamide CAS 321571-51-1

Purity 97%+In StockPharmaceutical Standards
CAS No.321571-51-1
Molecular FormulaC18H16ClN3O
Molecular Weight325.79 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-Benzyl-4-chloro-1-(4-methylphenyl)-1H-pyrazole-5-carboxamide CAS 321571-51-1 chemical structure

Description

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

CATO supplies N-Benzyl-4-chloro-1-(4-methylphenyl)-1H-pyrazole-5-carboxamide (CAS 321571-51-1), a certified reference material (molecular formula C18H16ClN3O, MW 325.79 g/mol) for analytical method development and quality control.

Owing to a steroid core, an amide group, a hydroxyl group, an ether linkage, chlorine substitution, N-Benzyl-4-chloro-1-(4-methylphenyl)-1H-pyrazole-5-carboxamide is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 325.79 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

Physical & Chemical Properties

Molecular FormulaC18H16ClN3O
Molecular Weight325.79 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentCl-containing
Nitrogen Atoms3

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